Masked polycythemia vera diagnosed according to WHO and BCSH classification.
about
Rationale for revision and proposed changes of the WHO diagnostic criteria for polycythemia vera, essential thrombocythemia and primary myelofibrosisManagement of polycythaemia vera: a critical review of current data.Current and future treatment options for polycythemia vera.Clinical impact of bone marrow morphology for the diagnosis of essential thrombocythemia: comparison between the BCSH and the WHO criteriaNovel insights into the biology and treatment of chronic myeloproliferative neoplasms.From leeches to personalized medicine: evolving concepts in the management of polycythemia vera.Anagrelide hydrochloride and ruxolitinib for treatment of polycythemia vera.How we diagnose and treat essential thrombocythaemia.Myeloproliferative neoplasms: A decade of discoveries and treatment advances.Myeloproliferative neoplasms: Morphology and clinical practice.European LeukemiaNet study on the reproducibility of bone marrow features in masked polycythemia vera and differentiation from essential thrombocythemia.Laboratory Investigation of Myeloproliferative Neoplasms (MPNs): Recommendations of the Canadian Mpn Group.Progression of primary myelofibrosis to polycythemia vera: A case report.Masked polycythaemia vera is genetically intermediate between JAK2V617F mutated essential thrombocythaemia and overt polycythaemia vera.From anemia to polycythemia in 4 weeks.Straightforward identification of masked polycythemia vera based on proposed revision of World Health Organization diagnostic criteria for BCR-ABL1-negative myeloproliferative neoplasms.JAK2V617F mutation status and allele burden in classical Ph-negative myeloproliferative neoplasms in Japan.Frequency of polycythemia in individuals with normal complete blood cell counts according to the new 2016 WHO classification of myeloid neoplasms.Comparison of JAK2(V617F) -positive essential thrombocythaemia and early primary myelofibrosis: The impact of mutation burden and histology.SOHO State-of-the-Art Update and Next Questions: MPN.Masked polycythaemia vera: presenting features, response to treatment and clinical outcomes.A lower intensity of treatment may underlie the increased risk of thrombosis in young patients with masked polycythaemia vera.Discriminating between essential thrombocythemia and masked polycythemia vera in JAK2 mutated patients.
P2860
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P2860
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@en
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@nl
type
label
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@en
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@nl
prefLabel
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@en
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@nl
P2093
P2860
P356
P1476
Masked polycythemia vera diagnosed according to WHO and BCSH classification.
@en
P2093
Alessandra Carobbio
Alessandro M Vannucchi
Alessandro Rambaldi
Bettina Gisslinger
Elisa Rumi
Guido Finazzi
Heinz Gisslinger
Jürgen Thiele
Leonhard Müllauer
Marco Ruggeri
P2860
P304
P356
10.1002/AJH.23617
P577
2014-02-01T00:00:00Z